CN1186124C - 一种复合型碱催化剂及其制备方法 - Google Patents
一种复合型碱催化剂及其制备方法 Download PDFInfo
- Publication number
- CN1186124C CN1186124C CNB031485669A CN03148566A CN1186124C CN 1186124 C CN1186124 C CN 1186124C CN B031485669 A CNB031485669 A CN B031485669A CN 03148566 A CN03148566 A CN 03148566A CN 1186124 C CN1186124 C CN 1186124C
- Authority
- CN
- China
- Prior art keywords
- hydroxide
- base catalyst
- alkali metal
- compound base
- tetraalkylammonium
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
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- 239000003054 catalyst Substances 0.000 title claims abstract description 58
- 239000002131 composite material Substances 0.000 title abstract description 27
- 238000000034 method Methods 0.000 title description 5
- 150000005621 tetraalkylammonium salts Chemical class 0.000 claims abstract description 17
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 17
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims abstract description 16
- 238000006243 chemical reaction Methods 0.000 claims abstract description 13
- 238000002360 preparation method Methods 0.000 claims abstract description 10
- 238000003756 stirring Methods 0.000 claims abstract description 9
- 229910044991 metal oxide Inorganic materials 0.000 claims abstract description 8
- 150000004706 metal oxides Chemical class 0.000 claims abstract description 8
- 239000002585 base Substances 0.000 claims description 28
- WGTYBPLFGIVFAS-UHFFFAOYSA-M tetramethylammonium hydroxide Chemical group [OH-].C[N+](C)(C)C WGTYBPLFGIVFAS-UHFFFAOYSA-M 0.000 claims description 22
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 17
- 150000005622 tetraalkylammonium hydroxides Chemical class 0.000 claims description 14
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 9
- 229910000272 alkali metal oxide Inorganic materials 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 6
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- KKCBUQHMOMHUOY-UHFFFAOYSA-N sodium oxide Chemical compound [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 claims description 4
- 229910001948 sodium oxide Inorganic materials 0.000 claims description 4
- 229940073455 tetraethylammonium hydroxide Drugs 0.000 claims description 4
- LRGJRHZIDJQFCL-UHFFFAOYSA-M tetraethylazanium;hydroxide Chemical compound [OH-].CC[N+](CC)(CC)CC LRGJRHZIDJQFCL-UHFFFAOYSA-M 0.000 claims description 4
- WJZPIORVERXPPR-UHFFFAOYSA-L tetramethylazanium;carbonate Chemical compound [O-]C([O-])=O.C[N+](C)(C)C.C[N+](C)(C)C WJZPIORVERXPPR-UHFFFAOYSA-L 0.000 claims description 4
- 150000005324 oxide salts Chemical class 0.000 claims description 2
- 229910001950 potassium oxide Inorganic materials 0.000 claims description 2
- KJFVITRRNTVAPC-UHFFFAOYSA-L tetramethylazanium;sulfate Chemical group C[N+](C)(C)C.C[N+](C)(C)C.[O-]S([O-])(=O)=O KJFVITRRNTVAPC-UHFFFAOYSA-L 0.000 claims description 2
- LPSKDVINWQNWFE-UHFFFAOYSA-M tetrapropylazanium;hydroxide Chemical compound [OH-].CCC[N+](CCC)(CCC)CCC LPSKDVINWQNWFE-UHFFFAOYSA-M 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims 2
- 239000007864 aqueous solution Substances 0.000 claims 1
- JKQOBWVOAYFWKG-UHFFFAOYSA-N molybdenum trioxide Chemical compound O=[Mo](=O)=O JKQOBWVOAYFWKG-UHFFFAOYSA-N 0.000 claims 1
- CHWRSCGUEQEHOH-UHFFFAOYSA-N potassium oxide Chemical compound [O-2].[K+].[K+] CHWRSCGUEQEHOH-UHFFFAOYSA-N 0.000 claims 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 claims 1
- LQNUZADURLCDLV-UHFFFAOYSA-N nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC=C1 LQNUZADURLCDLV-UHFFFAOYSA-N 0.000 abstract description 31
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 abstract description 20
- 239000003513 alkali Substances 0.000 abstract description 10
- 238000006482 condensation reaction Methods 0.000 abstract description 5
- 239000000047 product Substances 0.000 abstract description 5
- 239000006227 byproduct Substances 0.000 abstract description 3
- 238000006467 substitution reaction Methods 0.000 abstract description 3
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract description 2
- 239000001257 hydrogen Substances 0.000 abstract description 2
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- 230000000269 nucleophilic effect Effects 0.000 abstract description 2
- 125000005207 tetraalkylammonium group Chemical group 0.000 abstract 3
- 150000001448 anilines Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 238000002156 mixing Methods 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- XXYMSQQCBUKFHE-UHFFFAOYSA-N 4-nitro-n-phenylaniline Chemical compound C1=CC([N+](=O)[O-])=CC=C1NC1=CC=CC=C1 XXYMSQQCBUKFHE-UHFFFAOYSA-N 0.000 description 4
- OIJHFHYPXWSVPF-UHFFFAOYSA-N para-Nitrosodiphenylamine Chemical compound C1=CC(N=O)=CC=C1NC1=CC=CC=C1 OIJHFHYPXWSVPF-UHFFFAOYSA-N 0.000 description 4
- 230000002194 synthesizing effect Effects 0.000 description 3
- OKIZCWYLBDKLSU-UHFFFAOYSA-M N,N,N-Trimethylmethanaminium chloride Chemical compound [Cl-].C[N+](C)(C)C OKIZCWYLBDKLSU-UHFFFAOYSA-M 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000004811 liquid chromatography Methods 0.000 description 2
- LQNUZADURLCDLV-IDEBNGHGSA-N nitrobenzene Chemical group [O-][N+](=O)[13C]1=[13CH][13CH]=[13CH][13CH]=[13CH]1 LQNUZADURLCDLV-IDEBNGHGSA-N 0.000 description 2
- VDZOOKBUILJEDG-UHFFFAOYSA-M tetrabutylammonium hydroxide Chemical compound [OH-].CCCC[N+](CCCC)(CCCC)CCCC VDZOOKBUILJEDG-UHFFFAOYSA-M 0.000 description 2
- GNGCALKASVBYMT-UHFFFAOYSA-N 2-nitroso-n-phenylaniline Chemical compound O=NC1=CC=CC=C1NC1=CC=CC=C1 GNGCALKASVBYMT-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Natural products C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 description 1
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000011552 falling film Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 150000007529 inorganic bases Chemical class 0.000 description 1
- ATGUVEKSASEFFO-UHFFFAOYSA-N p-aminodiphenylamine Chemical compound C1=CC(N)=CC=C1NC1=CC=CC=C1 ATGUVEKSASEFFO-UHFFFAOYSA-N 0.000 description 1
- 125000001791 phenazinyl group Chemical class C1(=CC=CC2=NC3=CC=CC=C3N=C12)* 0.000 description 1
- NOTVAPJNGZMVSD-UHFFFAOYSA-N potassium oxide Chemical class [K]O[K] NOTVAPJNGZMVSD-UHFFFAOYSA-N 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- APBDREXAUGXCCV-UHFFFAOYSA-L tetraethylazanium;carbonate Chemical compound [O-]C([O-])=O.CC[N+](CC)(CC)CC.CC[N+](CC)(CC)CC APBDREXAUGXCCV-UHFFFAOYSA-L 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Description
Claims (12)
Priority Applications (31)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031485669A CN1186124C (zh) | 2003-07-04 | 2003-07-04 | 一种复合型碱催化剂及其制备方法 |
US10/883,042 US7084302B2 (en) | 2003-07-04 | 2004-07-02 | Process for preparing 4-aminodiphenylamine |
JP2006517937A JP4546958B2 (ja) | 2003-07-04 | 2004-07-02 | 4−アミノジフェニルアミンの製造方法 |
ES04738331T ES2298762T3 (es) | 2003-07-04 | 2004-07-02 | Proceso para preparar 4-aminodifenilamina. |
US10/882,677 US7176333B2 (en) | 2003-07-04 | 2004-07-02 | Process for preparing 4-aminodiphenylamine |
ES04738332T ES2373720T3 (es) | 2003-07-04 | 2004-07-02 | Método para la producción de 4-aminodifenilamina. |
EA200600052A EA009396B1 (ru) | 2003-07-04 | 2004-07-02 | Способ получения 4-аминодифениламина |
EP04738332A EP1645555B1 (en) | 2003-07-04 | 2004-07-02 | A method for producing 4-aminodiphenylamine |
EP04738331A EP1591438B1 (en) | 2003-07-04 | 2004-07-02 | A process for preparing 4-aminodiphenylamine |
BRPI0412101-5A BRPI0412101A (pt) | 2003-07-04 | 2004-07-02 | processo para a preparação da 4-aminodifenilamina |
CA2515238A CA2515238C (en) | 2003-07-04 | 2004-07-02 | Process for preparing 4-aminodiphenylamine |
PL04738332T PL1645555T3 (pl) | 2003-07-04 | 2004-07-02 | Sposób wytwarzania 4-aminodifenyloaminy |
JP2006500463A JP4500302B2 (ja) | 2003-07-04 | 2004-07-02 | 4−アミノジフェニルアミンの製造方法 |
PCT/CN2004/000734 WO2005003079A1 (fr) | 2003-07-04 | 2004-07-02 | Procede de production d'une 4-aminodiphenylamine |
KR1020040051541A KR100612922B1 (ko) | 2003-07-04 | 2004-07-02 | 4-아미노 디페닐아민의 제조방법 |
AT04738332T ATE526305T1 (de) | 2003-07-04 | 2004-07-02 | Verfahren zur herstellung von 4-aminodiphenylamin |
CA2531074A CA2531074C (en) | 2003-07-04 | 2004-07-02 | Process for preparing 4-aminodiphenylamine |
PCT/CN2004/000733 WO2005003078A1 (en) | 2003-07-04 | 2004-07-02 | A process for preparing 4-aminodiphenylamine |
PT04738332T PT1645555E (pt) | 2003-07-04 | 2004-07-02 | Um método para produzir 4-aminodifenilamina |
EA200501647A EA009395B1 (ru) | 2003-07-04 | 2004-07-02 | Способ получения 4-аминодифениламина |
MXPA05013788A MXPA05013788A (es) | 2003-07-04 | 2004-07-02 | Proceso para preparar 4-aminodifenilamina. |
DE602004010234T DE602004010234T2 (de) | 2003-07-04 | 2004-07-02 | Verfahren zur herstellung von 4-aminodiphenylamin |
KR1020040051932A KR100612923B1 (ko) | 2003-07-04 | 2004-07-05 | 4-아미노 디페닐아민의 제조방법 |
US11/477,954 US7235694B2 (en) | 2003-07-04 | 2006-06-30 | Process for preparing 4-aminodiphenylamine |
US11/757,277 US20080039657A1 (en) | 2003-07-04 | 2007-06-01 | Process for preparing 4-aminodiphenylamine |
US11/759,901 US20070227675A1 (en) | 2003-07-04 | 2007-06-07 | Process for preparing 4-aminodiphenylamine |
US11/759,897 US8293673B2 (en) | 2003-07-04 | 2007-06-07 | Process for preparing 4-aminodiphenylamine |
US12/195,371 US7989662B2 (en) | 2003-07-04 | 2008-08-20 | Process for preparing 4-aminodiphenylamine |
US12/900,459 US8486223B2 (en) | 2003-07-04 | 2010-10-07 | Falling film evaporator |
US13/104,900 US8686188B2 (en) | 2003-07-04 | 2011-05-10 | Process for preparing 4-aminodiphenylamine |
US13/620,588 US9029603B2 (en) | 2003-07-04 | 2012-09-14 | Process for preparing alkylated p-phenylenediamines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031485669A CN1186124C (zh) | 2003-07-04 | 2003-07-04 | 一种复合型碱催化剂及其制备方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1470330A CN1470330A (zh) | 2004-01-28 |
CN1186124C true CN1186124C (zh) | 2005-01-26 |
Family
ID=34156271
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB031485669A Expired - Lifetime CN1186124C (zh) | 2003-07-04 | 2003-07-04 | 一种复合型碱催化剂及其制备方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1186124C (zh) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100336796C (zh) * | 2004-07-15 | 2007-09-12 | 王农跃 | 制备4-氨基二苯胺的方法 |
CN100453525C (zh) * | 2004-07-15 | 2009-01-21 | 江苏圣奥化学科技有限公司 | 制备4-氨基二苯胺的方法 |
CN108558675A (zh) * | 2018-04-25 | 2018-09-21 | 南通理工学院 | 一种4-氨基二苯胺的合成方法 |
-
2003
- 2003-07-04 CN CNB031485669A patent/CN1186124C/zh not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
CN1470330A (zh) | 2004-01-28 |
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Legal Events
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C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
ASS | Succession or assignment of patent right |
Owner name: SHANDONG SHENG AO CHEMICAL CO., LTD. Free format text: FORMER OWNER: GUO ZHANGYU Effective date: 20080118 |
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C41 | Transfer of patent application or patent right or utility model | ||
TR01 | Transfer of patent right |
Effective date of registration: 20080118 Address after: 1#, North Ring Road, Heze, Shandong, Caoxian Patentee after: Shandong Sinorgchem chemical Limited by Share Ltd. Address before: 1#, North Ring Road, Heze, Shandong, Caoxian Patentee before: Guo Changyu |
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ASS | Succession or assignment of patent right |
Owner name: JIANGSU SHENG AO CHEMICAL TECHNOLOGY CO., LTD. Free format text: FORMER OWNER: SHANDONG SHENG AO CHEMICAL CO., LTD. Effective date: 20080711 |
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C41 | Transfer of patent application or patent right or utility model | ||
TR01 | Transfer of patent right |
Effective date of registration: 20080711 Address after: Room 1, No. 212, drug City Avenue, Jiangsu, Taizhou Patentee after: Jiangsu Sinorgchem Technology Co.,Ltd. Address before: No. 1, North Ring Road, Heze, Shandong, Caoxian Patentee before: Shandong Sinorgchem chemical Limited by Share Ltd. |
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CP03 | Change of name, title or address | ||
CP03 | Change of name, title or address |
Address after: Room 1, building 606, medicine City Avenue, Jiangsu, Taizhou, China, 225316 Patentee after: SENNICS Co.,Ltd. Address before: 225300 Jiangsu City, Taizhou Province medicine city road, room 1, No. 212 Patentee before: Jiangsu Sinorgchem Technology Co.,Ltd. |
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CP02 | Change in the address of a patent holder | ||
CP02 | Change in the address of a patent holder |
Address after: 200120 Shanghai, China (Shanghai) free trade zone, 2304 Pudong Avenue, 2304. Patentee after: SENNICS Co.,Ltd. Address before: 225316 Room 606, medicine City Avenue, Taizhou, Taizhou, Jiangsu Patentee before: SENNICS Co.,Ltd. |
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CX01 | Expiry of patent term |
Granted publication date: 20050126 |
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CX01 | Expiry of patent term |